DANIELLE DELUCY

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Recording

FDA Case Scenarios – Best Practices for Managing Inspection Situations

Duration: 75 Minutes

DANIELLE DELUCY
FDB2169
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Recording

How to conduct Annual Product Reviews to achieve GMP Compliance

Duration: 75 Minutes

DANIELLE DELUCY
FDB3164
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Recording

Good Documentation Practices

Duration: 75 Minutes

DANIELLE DELUCY
FDB2866
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Recording

Steam Sterilization Microbiology and Autoclave Performance Qualification

Duration: 75 Minutes

DANIELLE DELUCY
FDB2261
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Recording

Effective Batch Record Review

Duration: 75 Minutes

DANIELLE DELUCY
FDB2469
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Recording

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

Duration: 3 Hour

DANIELLE DELUCY
FDB3384
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Recording

Effective Standard Operating Procedure (SOPs) Development for Regulatory Compliance

Duration: 75 Minutes

DANIELLE DELUCY
FDB1868
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Recording

GMP Data Integrity – Implementation and Management

Duration: 75 Minutes

DANIELLE DELUCY
FDB1869
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Recording

Investigating Deviations – Best Practices

Duration: 75 Minutes

DANIELLE DELUCY
FDB1860
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Recording

Robust CAPA and Proper Root Cause Analysis

Duration: 75 Minutes

DANIELLE DELUCY
FDB2165
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Recording

How to Properly Investigate OOS Results

Duration: 75 Minutes

DANIELLE DELUCY
FDB2166
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Recording

How To Properly Manage a Regulatory Inspection

Duration: 75 Minutes

DANIELLE DELUCY
FDB2266
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Recording

How to Conduct Successful Supplier Audits

Duration: 75 Minutes

DANIELLE DELUCY
FDB2164
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Recording

Proper Root Cause Analysis

Duration: 75 Minutes

DANIELLE DELUCY
FDB2466
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Recording

Sunshine Act Reporting – Clarification for Clinical Research

Duration: 75 Minutes

DANIELLE DELUCY
FDB3162
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Recording

Achieving Compliance with Proper CAPA Systems

Duration: 60 Minutes

DANIELLE DELUCY
FDB2862
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Recording

Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations

Duration: 75 Minutes

DANIELLE DELUCY
FDB2461
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Recording

Successful Deviation Investigations

Duration: 60 Minutes

DANIELLE DELUCY
FDB2462
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Recording

Guideline to Aseptic Technique and Clean Room Behavior

Duration: 75 Minutes

DANIELLE DELUCY
FDB2463
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Recording

Laboratory Controls – Anticipate the Systems Based FDA Inspection

Duration: 75 Minutes

DANIELLE DELUCY
FDB2467
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Recording

Process Validation LifeCycle

Duration: 75 Minutes

DANIELLE DELUCY
FDB2468
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Recording

Conducting Successful Quality Audits

Duration: 75 Minutes

DANIELLE DELUCY
FDB2863
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Recording

Biosafety and Blood borne Pathogen Safety in the Lab

Duration: 75 Minutes

DANIELLE DELUCY
FDB2861
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Recording

Understanding Aseptic Technique and Cleanroom Behavior – Avoiding Human Error

Duration: 75 Minutes

DANIELLE DELUCY
FDB2865
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Recording

Successful Change Control Management

Duration: 75 Minutes

DANIELLE DELUCY
FDB2868
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Recording

3-Hour Virtual Seminar on Successful Deviation Investigations

Duration: 3 Hour

DANIELLE DELUCY
FDB3081
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Recording

Critical Elements Of Quality Risk Management Relating to FDA Compliance

Duration: 75 Minutes

DANIELLE DELUCY
FDB2262
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Recording

Effective Standard Operating Procedure (SOPs) Development

Duration: 75 Minutes

DANIELLE DELUCY
FDB3161
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Recording

3-Hour Virtual Seminar On Batch Record Review And Product Release

Duration: 3 Hour

DANIELLE DELUCY
FDB3282
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Recording

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

Duration: 3 Hour

DANIELLE DELUCY
FDB3384
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Recording

Step-By-Step Process For Successful Sterility Failure Investigations

Duration: 60 Minutes

DANIELLE DELUCY
FDB2465